IQVIA in Low Bradley, United Kingdom, is looking for experienced Clinical Research Associates to perform site monitoring visits, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. Candidates should have at least 1 year of independent on-site monitoring experience in interventional studies.
The role involves evaluating study site practices, tracking regulatory submissions, and maintaining effective communication with team members and sites. Please note this position is not eligible for UK visa sponsorship.
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